BEUDAMED
    8 results · 24ms · Sources: EU EUDAMED, US FDA

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    IMPLEX HEDROCEL REPLACEMENT CUP INSERT MODEL NUMBERS 02-246-XXYYY, 02-247-XXYYY, 02-248-XXYYY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Polystar Selection EDITION HD

    FDA UDI
    Merz Dental GmbH·D7091983128·posteriors; shade BL1; size XL; upper jaw

    STANBIO ENZYMATIC UREA NITROGEN DETERMINAT #2010

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    EnSite Velocity Cardiac Mapping System v5.2, EnSite Precision Cardiac Mapping System v2.2

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN DEPUY PINNACLE METAL LINER

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code KWA·February 28, 2013

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·February 4, 2011

    PLUMSET CLAVE PORT CLAVE SITE 103IN NDHP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 2, 2014

    BIOMET MICROFIXATION MANDIBULAR FRACTURE/ RECONSTRUCTION DEVICES

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·June 3, 2016